A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200512



Internal ID20767552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155080703..155146082hg38UCSC Ensembl
chr1:155053179..155118558hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3865380
hg1965380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332159
Supporting Variants
Samples
Known GenesDPM3, EFNA1, EFNA3, SLC50A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200512
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer